| Identification | Back Directory | [Name]
5-Methyl-3-vinyl-2-oxazolidinone | [CAS]
3395-98-0 | [Synonyms]
5-Methyl-3-vinyl-2-oxazolidinone
5-Methyl-3-vinyloxazolidin-2-one
3-Ethenyl-5-methyl-2-oxazolidinone
2-Oxazolidinone, 3-ethenyl-5-methyl- | [EINECS(EC#)]
809-852-5 | [Molecular Formula]
C6H9NO2 | [MDL Number]
MFCD34167271 | [MOL File]
3395-98-0.mol | [Molecular Weight]
127.14 |
| Chemical Properties | Back Directory | [Boiling point ]
78-81 °C(Press: 1.3 Torr) | [density ]
1.085 g/cm3 | [vapor pressure ]
2.2-25Pa at 20-50℃ | [pka]
-0.39±0.40(Predicted) | [PH]
7.5 at 20℃ and 10g/L | [InChI]
InChI=1S/C6H9NO2/c1-3-7-4-5(2)9-6(7)8/h3,5H,1,4H2,2H3 | [InChIKey]
HXFNRRNDWNSKFM-UHFFFAOYSA-N | [SMILES]
O1C(C)CN(C=C)C1=O | [LogP]
0.8 at 23℃ and pH6.3 |
| Hazard Information | Back Directory | [Uses]
5-Methyl-3-vinyl-2-oxazolidinone (VMOX) is a relatively new commercial monomer used as a reactive diluent in UV curing products such as adhesives, coatings, and inks.2
| [structure and hydrogen bonding]
The 5-methyl-3-vinyl-2-oxazolidinone (VMOX) structure resembles the VP monomer with a 5-membered heterocyclic ring and good hydrogen-bonding capability.1
| [References]
[1] Kelland*, M. A., Dirdal, E. G., Ghosh, R., & Ajiro, H. (2023). Improved Gas Hydrate Kinetic Inhibition for 5-Methyl-3-vinyl-2-oxazolidinone Copolymers and Synergists. ACS Omega, 8 31, 28859–28865. https://doi.org/10.1021/acsomega.3c03986
[2] Kelland*, M. A., Dirdal, E. G., Ghosh, R., & Ajiro, H. (2022). 5-Methyl-3-vinyl-2-oxazolidinone–Investigations of a New Monomer for Kinetic Hydrate Inhibitor Polymers. Energy & Fuels, 36 5, 2609–2615. https://doi.org/10.1021/acs.energyfuels.1c04417
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